Identifying Mitochondrial Disease: Case studies (Webinar)
|When||Tuesday, 13 September @ 7:00 pm - 7:30 pm AEST|
|Where||Online via Zoom|
Diagnosing primary mitochondrial disease or ‘mito’ can be challenging due to the wide variety of symptoms and sub-groups. Many experts refer to it as the ‘notorious masquerader’ because it mimics many other illnesses. Join metabolic geneticist Dr Shanti Balasubramaniam to explore the multiple organ systems involved in mito and identify “red flag” symptoms. Paediatric and adult clinical cases will be presented to illustrate how GPs have an important role to play in identifying a suspected diagnosis of mito.
Register now for the opportunity to submit your clinical question. Join us live for an interactive discussion or receive the link to the recording after the event. Dr Balasubramaniam will present for approximately 20 minutes, followed by an interactive Q&A.
Presented by the Mito Foundation
Contact information: Emma Celis email@example.com
Additional information/resources: On average, 10 out of every 2,000 patients seen at a general practice have mitochondrial DNA mutations, which may lead to mitochondrial disease or disease involving mitochondrial dysfunction. Let us help you provide them with evidence-based care and resources. Visit the Maybe It's Mito GP education page.